Multistep synthesis of a new tricyclic azaindole-based scaffold

Autor:	Mauro Angiolini, Andrea Lombardi Borgia, Tiziano Bandiera
Rok vydání:	2009
Předmět:	chemistry.chemical_classification Scaffold Stereochemistry Organic Chemistry chemistry.chemical_element Ring (chemistry) Biochemistry chemistry Intramolecular force Heck reaction Drug Discovery Moiety Tricyclic Palladium
Zdroj:	Tetrahedron Letters. 50:5156-5158
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2009.06.126
Popis:	In this Letter the synthetic pathway adopted for the preparation of a new functionalized tricyclic scaffold containing the 7-azaindole moiety is presented. An intramolecular palladium-mediated reaction is described as the crucial step for a condensed seven-membered ring formation.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::fa5fef12944e26baa6a34b0486baacaf https://doi.org/10.1016/j.tetlet.2009.06.126 Zobrazit plný text záznamu Full Text from ScienceDirect